FDA NDC Directory · JSON-LD · Markdown

PROPOFOL

NDC 80830-2364 · HUMAN PRESCRIPTION DRUG · INJECTION, EMULSION

Generic namepropofol
Labeler / ManufacturerAmneal Pharmaceuticals Private Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA217525
Dosage form / routeINJECTION, EMULSION · INTRAVENOUS
Active ingredientsPROPOFOL (10 mg/mL)
Marketing started20240816
Package count1

External sources

Source: openFDA. Public-domain (CC0).